A comparative study about recovery from being completely unconscious and only losing sensation at operative area in patients undergoing abdominal surgeries through minimal cut

Comparison of Quality of Recovery between General Anaesthesia and Thoracic Spinal Anaesthesia in patients undergoing laparoscopic abdominal surgery: A single blinded randomised controlled trial - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/10/074615

Enrollment

Registered

2024-10-03

Start date

Unknown

Completion date

Unknown

Last updated

2024-10-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Thoracic Spinal Anaesthesia: Patients will receive Thoracic Spinal Anaesthesia in the form of intrathecal catheter with Ketamine, preservative free Midazolam and isobaric Levobupivacain

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anaesthesiologists (ASA) grade I-III patients undergoing elective laparoscopic/robotic abdominal surgeries

Exclusion criteria

Exclusion criteria: Patients with informed refusal Patients undergoing emergency and open abdominal surgeries Patients with severe medical illnesses (ASA IV-V grade) Patients with known allergy to anaesthestic drugs Patients having absolute/relative contraindications to spinal anaesthesia Pregnant patients

Design outcomes

Secondary

Measure	Time frame
Assessment of in house mortality following surgeryTimepoint: At 30 and 90 days after surgery;Compare the Length of Stay (LoS) in the hospitalTimepoint: From the date of Admission (DoA) to Date of Discharge (DoD);Compare the Post Anaesthesia Cre Unit (PACU) stay by using modified Aldrete scoreTimepoint: At every 15 minutes intervals after surgery gets over till patients get discharged from PACU;To compare how satisfied patients areTimepoint: 24 hours of postsurgical timeline;To compare how satisfied surgeons areTimepoint: Baseline at the end of surgery;To look for any in house new onset morbidityTimepoint: Upto 3 months following surgery;To note the percentage conversion to General AnaesthesiaTimepoint: Baseline at the end of surgery	—

Measure

Time frame

Assessment of in house mortality following surgeryTimepoint: At 30 and 90 days after surgery;Compare the Length of Stay (LoS) in the hospitalTimepoint: From the date of Admission (DoA) to Date of Discharge (DoD);Compare the Post Anaesthesia Cre Unit (PACU) stay by using modified Aldrete scoreTimepoint: At every 15 minutes intervals after surgery gets over till patients get discharged from PACU;To compare how satisfied patients areTimepoint: 24 hours of postsurgical timeline;To compare how satisfied surgeons areTimepoint: Baseline at the end of surgery;To look for any in house new onset morbidityTimepoint: Upto 3 months following surgery;To note the percentage conversion to General AnaesthesiaTimepoint: Baseline at the end of surgery

—

Primary

Measure	Time frame
Quality of Recovery following surgeryTimepoint: At 24 hours after surgery	—

Countries

India

Contacts

Public ContactDr Praveen Talawar

All India Institute of Medical Sciences (AIIMS), Rishikesh

praveenrt64@gmail.com9654162941

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026